dimethyl fumarate
- Product NDC
- 70771-1532
- 11-digit product format
- 707711532
- Labeler code
- 70771
- Product ID
- 70771-1532_71df19ca-2bf4-489c-a411-ee237d511b8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dimethyl fumarate
- Dosage form
- KIT
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA210538
- Marketing category
- ANDA
- Marketing start
- 2020-09-28
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70771-1532-3 | dimethyl fumarate | 1 in 1 KIT | KIT | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1532 | DIMETHYL FUMARATE (DIMETHYL FUMARATE) KIT DIMETHYL FUMARATE CAPSULE, DELAYED RELEASE [ZYDUS LIFESCIENCES LIMITED] | 5 | Legacy NDC, 1 package rows | 20250403_7203a262-de0f-42dd-b4fb-8856758b82e9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1532-3 | 70771153203 | 1 KIT in 1 KIT (70771-1532-3) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 kit | 2020-09-28 | 0000-00-00 | No | No | Current |